N-(3-cyano-5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl)-3,4,5-trihydroxybenzamide

ID: ALA5220303

Chembl Id: CHEMBL5220303

PubChem CID: 139593814

Max Phase: Preclinical

Molecular Formula: C15H12N2O4S

Molecular Weight: 316.34

Associated Items:

Names and Identifiers

Canonical SMILES:  N#Cc1c(NC(=O)c2cc(O)c(O)c(O)c2)sc2c1CCC2

Standard InChI:  InChI=1S/C15H12N2O4S/c16-6-9-8-2-1-3-12(8)22-15(9)17-14(21)7-4-10(18)13(20)11(19)5-7/h4-5,18-20H,1-3H2,(H,17,21)

Standard InChI Key:  WZXZAQCXHPVIED-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5220303

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Associated Targets(Human)

HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Staphylococcus coagulans (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Heyndrickxia coagulans (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Proteus vulgaris (5823 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 316.34Molecular Weight (Monoisotopic): 316.0518AlogP: 2.48#Rotatable Bonds: 2
Polar Surface Area: 113.58Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 7.62CX Basic pKa: CX LogP: 3.10CX LogD: 2.90
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.64Np Likeness Score: -1.55

References

1. Duvauchelle V, Meffre P, Benfodda Z..  (2022)  Recent contribution of medicinally active 2-aminothiophenes: A privileged scaffold for drug discovery.,  238  [PMID:35696863] [10.1016/j.ejmech.2022.114502]
2. Al Zahrani NA, El-Shishtawy RM, Asiri AM..  (2020)  Recent developments of gallic acid derivatives and their hybrids in medicinal chemistry: A review.,  204  [PMID:32731188] [10.1016/j.ejmech.2020.112609]

Source